2015•Translational gastrointestinal cancerRequires access

Effect and mechanism of inhibiting ZNF139 on apoptosis in human gastric cancer cell line BGC823

Li-Qiao Fan, Bibo Tan, Yong Li, Qun Zhao, Yü Liu, Dong Hua Wang, Zhidong Zhang

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Abstract

Objective: To investigate the role of ZNF139 played in GC cell apoptosis and to explore its mechanism. Methods: Expression of ZNF139 in GC tissues, adjacent normal tissues, GC cell lines MKN28, SGC7901, BGC823 and in gastric epithelial cell line GES-1 were tested. Then ZNF139-specific siRNA was transfected into BGC823 cells. Viability, cell cycle and apoptosis of GC cells were detected. Survivin, x-IAP, caspase-3, Fas, p53, Bcl-2 and Bax genes were detected. Results: The results showed that ZNF139 was highly expressed in gastric cancer tissues and cells. FCM indicated that after transfection, GC cells in G0/G1 phase was significantly increased, and those cells was significantly reduced in G2/M phases after transfection, apoptosis rate of BGC823 cells was increased significantly. After ZNF139- siRNA was transfected into BGC823, QPCR and Western blot showed that expressions of Survivin, x-IAP and Bcl- 2 were significantly down-regulated, while expressions of caspase-3 and Bax were significantly up-regulated. Conclusion: ZNF139 functions to promote apoptosis resistance of BGC823.

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What this paper is about

Objective: To investigate the role of ZNF139 played in GC cell apoptosis and to explore its mechanism. Methods: Expression of ZNF139 in GC tissues, adjacent normal tissues, GC cell lines MKN28, SGC7901, BGC823 and in gastric epithelial cell line GES-1 were tested. Then ZNF139-specific siRNA was transfected into BGC823 cells. Viability, cell cycle and apoptosis of GC cells were detected. Survivin, x-IAP, caspase-3, Fas, p53, Bcl-2 and Bax genes were detected. Results: The results showed that ZNF139 was highly expressed in gastric cancer tissues and cells. FCM indicated that after transfection, GC cells in G0/G1 phase was significantly increased, and those cells was significantly reduced in G2/M phases after transfection, apoptosis rate of BGC823 cells was increased significantly. After ZNF139- siRNA was transfected into BGC823, QPCR and Western blot showed that expressions of Survivin, x-IAP and Bcl- 2 were significantly down-regulated, while expressions of caspase-3 and Bax were significantly up-regulated. Conclusion: ZNF139 functions to promote apoptosis resistance of BGC823.

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Available abstract

Objective: To investigate the role of ZNF139 played in GC cell apoptosis and to explore its mechanism. Methods: Expression of ZNF139 in GC tissues, adjacent normal tissues, GC cell lines MKN28, SGC7901, BGC823 and in gastric epithelial cell line GES-1 were tested. Then ZNF139-specific siRNA was transfected into BGC823 cells. Viability, cell cycle and apoptosis of GC cells were detected. Survivin, x-IAP, caspase-3, Fas, p53, Bcl-2 and Bax genes were detected. Results: The results showed that ZNF139 was highly expressed in gastric cancer tissues and cells. FCM indicated that after transfection, GC cells in G0/G1 phase was significantly increased, and those cells was significantly reduced in G2/M phases after transfection, apoptosis rate of BGC823 cells was increased significantly. After ZNF139- siRNA was transfected into BGC823, QPCR and Western blot showed that expressions of Survivin, x-IAP and Bcl- 2 were significantly down-regulated, while expressions of caspase-3 and Bax were significantly up-regulated. Conclusion: ZNF139 functions to promote apoptosis resistance of BGC823.

Key concepts: Survivin, Transfection, Apoptosis, Molecular biology, Cell culture, Cell cycle, Cell, Western blot

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